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Synthesis of some new azoles and their fused derivatives with anticipated biological activity / Doha Samir Mohamed Okpy ; Supervised Mohamed Ahmed Badawy , Nadia Hanafy Metwally ,

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Doha Samir Mohamed Okpy , 2014Description: 152 P. ; 25cmOther title:
  • تشييد بعض الأزولات الجديدة ومشتقاتها الملتحمة ذات نشاط بيولوجى متوقع [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry Summary: The original work of this thesis includes TWO research parts: The first part:- Studies the reactions of 5-ethoxymethylene-2-thioxo-4-thiazolidinone with ethyl glycinate and ethyl hydrazine carboxylate to afford imidazo[2,1-b]thiazoledione derivative and hydrazine carboxylate derivative of 2-thioxo-4-thiazolidinone respectively. The condensation of 5-(amino-methylene)-2-thioxo-4-thiazolidinone with different aromatic aldehydes in presence of piperidine as a basic catalyst afforded Z-5-(piperidin-1-ylmethylene)-2-thioxo-4-thiazolidinone. The alkaline hydrolysis of 5-aryl methylene)-2-thioxo-4-thiazolidinone affords 3-aryl-2-mercaptoacrylic acid derivatives, the latter compounds react with different {uF061}-arylhydrazono-malononitriles and trichloroacetonitrile to afford the corresponding thiazole derivatives. The structure for selected compounds was confirmed by X-ray crystallography
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.M.Sc.2014.Do.S (Browse shelf(Opens below)) Not for loan 01010110064015000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.M.Sc.2014.Do.S (Browse shelf(Opens below)) 64015.CD Not for loan 01020110064015000

Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry

The original work of this thesis includes TWO research parts: The first part:- Studies the reactions of 5-ethoxymethylene-2-thioxo-4-thiazolidinone with ethyl glycinate and ethyl hydrazine carboxylate to afford imidazo[2,1-b]thiazoledione derivative and hydrazine carboxylate derivative of 2-thioxo-4-thiazolidinone respectively. The condensation of 5-(amino-methylene)-2-thioxo-4-thiazolidinone with different aromatic aldehydes in presence of piperidine as a basic catalyst afforded Z-5-(piperidin-1-ylmethylene)-2-thioxo-4-thiazolidinone. The alkaline hydrolysis of 5-aryl methylene)-2-thioxo-4-thiazolidinone affords 3-aryl-2-mercaptoacrylic acid derivatives, the latter compounds react with different {uF061}-arylhydrazono-malononitriles and trichloroacetonitrile to afford the corresponding thiazole derivatives. The structure for selected compounds was confirmed by X-ray crystallography

Issued also as CD

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